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Aminoalkylphosphonates and related compounds as edg receptor agonists

a technology of edg receptor and aminoalkylphosphonates, which is applied in the direction of phosphorus organic compounds, peptide/protein ingredients, capsule delivery, etc., can solve the problems of gastrointestinal discomfort, nephrotoxicity, neurotoxicity, etc., and achieves the effect of reducing the number of side effects, and improving the effect of edg receptor activity

Inactive Publication Date: 2005-05-19
DOHERTY GEORGE A +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Anti-inflammatory agents such as NSAIDs act principally by blocking the effect or secretion of these mediators but do nothing to modify the immunologic basis of the disease.
Though they are effective in delaying or suppressing transplant rejection, Cyclosporin A and FK-506 are known to cause several undesirable side effects including nephrotoxicity, neurotoxicity, and gastrointestinal discomfort.

Method used

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  • Aminoalkylphosphonates and related compounds as edg receptor agonists
  • Aminoalkylphosphonates and related compounds as edg receptor agonists
  • Aminoalkylphosphonates and related compounds as edg receptor agonists

Examples

Experimental program
Comparison scheme
Effect test

example 1

(±)-2-Amino-4-(4-(octylphenyl))butanol, O-phosphate

Step A: (±)-2-Amino-4-(4-octylphenyl)butanoic acid

[0098] A mixture of 13.25 g (30.6 mmol) of diethyl 2-acetamido-2-(2-(4-octylphenyl)ethyl)propandioate (prepared according to the procedure described by Durand, et.al., Synthesis, 2000, 505-506, which is hereby incorporated by reference in its entirety) and 75 mL of concentrated HCL were stirred at 100° C. for 16 h. The mixture was cooled and 75 g of ice was added. The mixture was neutralized (pH=7) with 5 N NaOH. The precipitate was filtered, rinsed with water and dried to afford 8.9 g of the title compound: HPLC B: 2.68 min; ESI-MS 292 (M+H).

Step B: (±)-2-Benzyloxycarbonylamido-4-(4-octylphenyl)butanoic acid

[0099] A solution of 510 mg (1.75 mmol) of (±)-2-amino-4-(4-octylphenyl)butanoic acid (from EXAMPLE 1, Step A) in 10 mL of 1:1 v / v dioxane / 1 N NaOH was treated with 0.25 mL (1.75 mmol) of benzyl chloroformate and the resulting mixture was stirred at rt for 2 h. The mixture wa...

example 2

(±)-trans-3-Amino-4-(4-octylphenyl)but-1-enyl phosphonic acid

Step A: (±)-2-(t-butoxycarbonylamido)-4-(4-octylphenyl)butanoic acid

[0103] A solution of 9.8 g (30.6 mmol) of (±)-2-amino-4-(4-octylphenyl)butanoic acid (from EXAMPLE 1, Step A) in 150 mL of 1:1 v / v dioxane / 1 N NaOH was treated with 10 g (45.8 mmol) of di-t-butyl dicarbonate and stirred at rt for 1 h. The mixture was partitioned between 550 mL of 10:1 v / v EtOAc / iPrOH and 200 mL of 1 N HCl. The organic layer was separated, dried and concentrated. Flash chromatography on a Biotage 75S cartridge using 4:1 v / v heptane / EtOAc (2.5 L), then 4:1 v / v heptane / EtOAc+1% HOAc (5 L) as the eluant afforded 12.0 g (100%) of the title compound: HPLC B: 4.82 min; ESI-MS 292 (M-BOC+H).

Step B: (±)-2-(t-Butoxycarbonylamido)-4-(4-octylphenyl)butanol

[0104] The title compound was prepared from (±)-2-(t-butoxycarbonylamido)-4-(4-octylphenyl)butanoic acid (from EXAMPLE 2, Step A) using a procedure analogous to that described in EXAMPLE 1, Step ...

example 3

(±)-3-Amino-4-(4-octylphenyl)butyl phosphonic acid

Step A: Diethyl (±)-3-(-butoxycarbonylamino)-4-(4-octylphenyl)butyl phosphonate

[0108] A mixture of 100 mg (0.2 mmol) of diethyl (±)-trans-3-(t-butoxycarbonylamido-4-(4-octylphenyl)but-1-enyl phosphonate (from EXAMPLE 2, Step D) and 40 mg of 10% palladium on carbon in 5 mL of EtOH was stirred under an atmosphere of H2 for 20 h. The catalyst was filtered and the filtrate concentrated to afford 100 mg (100%) of the title compound.

Step B: (±)-3-Amino-4-(4-octylphenyl)butyl phosphonic acid

[0109] A solution of 100 mg (0.2 mmol) of diethyl (±)-3-(-butoxycarbonylamino)-4-(4octylphenyl)butyl phosphonate (from EXAMPLE 3, Step A) in 3 mL of CH2Cl2 was treated with 0.11 mL (0.77 mmol) of iodotrimethylsilane and stirred at rt for 1 h. The reaction was quenched with 5 mL of MeOH, then concentrated. HPLC purification (HPLC C) afforded 39 mg (56%) of the title compound: HPLC A: 3.94 min; HPLC B: 2.88 min; ESI-MS 356 (M+H).

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Abstract

The present invention encompasses compounds of formula (II); as well as the pharmaceutically acceptable salts and hydrates thereof. The compounds are useful for treating immune mediated diseases and conditions, such as bone marrow, organ and tissue transplant rejection. Pharmaceutical compositions and methods of use are included.

Description

BACKGROUND OF THE INVENTION [0001] The present invention is related to compounds that are S1P1 / Edg1 receptor agonists and thus have immunosuppressive activities by producing lymphocyte sequestration in secondary lymphoid tissues. The invention is also directed to pharmaceutical compositions containing such compounds and methods of treatment or prevention. [0002] Immunosuppressive agents have been shown to be useful in a wide variety of autoimmune and chronic inflammatory diseases, including systemic lupus erythematosis, chronic rheumatoid arthritis, type I diabetes mellitus, inflammatory bowel disease, biliary cirrhosis, uveitis, multiple sclerosis and other disorders such as Crohn's disease, ulcerative colitis, bullous pemphigoid, sarcoidosis, psoriasis, autoimmune myositis, Wegener's granulomatosis, ichthyosis, Graves ophthalmopathy, atopic dermatitis and asthma. They have also proved useful as part of chemotherapeutic regimens for the treatment of cancers, lymphomas and leukemias...

Claims

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Application Information

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IPC IPC(8): A61K31/18A61K31/197A61K31/41A61K31/4164A61K31/4192A61K31/4196A61K31/661A61K31/662A61P1/02A61P1/04A61P1/16A61P1/18A61P3/04A61P3/10A61P5/14A61P7/06A61P9/10A61P11/06A61P13/12A61P17/00A61P17/06A61P17/10A61P17/14A61P19/10A61P21/04A61P25/00A61P25/06A61P27/02A61P27/16A61P29/00A61P31/04A61P31/14A61P31/18A61P31/20A61P35/00A61P35/02A61P37/02A61P37/06A61P37/08C07C229/34C07C233/11C07C309/24C07C311/51C07D233/84C07D249/04C07D249/12C07D257/04C07D257/06C07F9/09C07F9/38
CPCA61K9/4825A61K31/66C07C229/34C07C309/24C07C311/51C07D233/84C07F9/3882C07D249/12C07D257/04C07D257/06C07F9/094C07F9/3808C07F9/3826C07D249/04A61P1/02A61P1/04A61P1/16A61P1/18A61P3/04A61P3/10A61P5/14A61P7/06A61P9/10A61P11/06A61P13/12A61P17/00A61P17/06A61P17/10A61P17/14A61P19/10A61P21/04A61P25/00A61P25/06A61P27/02A61P27/16A61P29/00A61P31/04A61P31/14A61P31/18A61P31/20A61P35/00A61P35/02A61P37/00A61P37/02A61P37/06A61P37/08
Inventor DOHERTY, GEORGE AHALE, JEFFREY J
Owner DOHERTY GEORGE A
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